drugset / Trial / NCT04679350

Efficacy and Safety of hzVSFv13 in Patients With COVID-19 Pneumonia

NCT04679350

Phase 2 Terminated 1 enrolled ImmuneMed, Inc.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

To explore the efficacy and confirm the safety of the concomitant administration of the standard of care and hzVSF-v13 in patients with COVID-19 infection

Timeline

Start
2021-03-18
Primary completion
2022-11-30
Completion
2022-12-30

Drugs

EvaluationDrugModalityDoseRoute
Subject Burfiralimab Monoclonal antibody 50 mg Intravenous
Subject Burfiralimab Monoclonal antibody 200 mg Intravenous

Indications